Canonical Allele Identifier: PA2828703902
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 14268
ClinVar RCV Id: RCV000015338 RCV000084543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364196.1:p.Lys257Met
CA225473
NM_001377267.1:c.770A>T